This frog is a common species that remains widespread throughout its historical habitat in western Washington, however, declines in British Columbia, Oregon, and California cause concern.
According to NatureServe, the state conservation status of the northern red-legged frog population is considered “apparently secure” in Washington.
Description and Range
Physical description
This is a medium-sized frog with a slender body, smooth skin, distinct dorsolateral folds, and an eye mask. Females can reach 4.2 inches snout to vent length and males 3.2 inches snout to vent length but in Washington females rarely exceed 3.5 inches and males rarely exceed 3 inches. The dorsal (topside) color is tan, brown, or olive-brown with varying amounts of black spotting and speckling. The undersides of the legs and margins of the abdomen are brick to orange-red; a gray wash may also be present. The legs are long. Mature males have gray swollen pads, called nuptial pads, on the thumbs. Juveniles resemble adults but may not have the red pigment on undersurfaces
The presence of dorsolateral folds distinguishes all native True Frogs (Ranid species) from other anurans in Washington State. All native True Frogs in western Washington are brownish colored frogs that are similar in general appearance. Cascades frogs are easily distinguished by the honey-yellow coloration on the abdomen and undersides of the legs.
The following northern red-legged frog traits distinguish them from Oregon and Columbia spotted frogs: 1) the groin is mottled with black and greenish yellow or cream-colored blotches, 2) distinct dorsolateral folds are present along the entire dorsal margins, 3) the eyes are oriented outward (laterally) so that only a portion of the pupil is visible when the frog is viewed from above, and 4) webbing is reduced between the toes so that the webbing on the longest toe does not extend past the first joint and the webbing is concave when the toes are pulled apart.
The exotic American bullfrog and exotic American green frog have a distinct fold (supratympanic fold) from the posterior edge of the eye, around the top of the external ear (tympanum) and ending at the shoulder; and typically have green coloration on the head.
Larvae
The tadpoles of the northern red-legged frog, Oregon spotted frogs, Columbia spotted frogs, and Cascades frogs are similar enough that distinguishing them is challenging.
The red-legged frog tadpole has an oval body with dorsal eyes. The tube for waste elimination (vent) is just right of the midline at the tail base, and the tube for moving respiratory water out of the body (spiracle) is on the upper middle left side. The dorsal fin terminates on the body at, or anterior to, the spiracle. The tail tip is pointed, and the dorsal fin is at least as high as the height of the tail musculature.
At hatching, tadpoles are dark brown but appear black in most light. They have long tails and short gills. As the larvae grow, the gills become concealed, the body color and belly lighten, and metallic flecks appear. In larger tadpoles, the ventral abdomen is often pinkish or yellowish and brassy flecks are visible on the sides. Tadpoles grow to 2 to 3 inches total length before metamorphosis.
Pacific treefrog tadpoles differ in having eyes along the outline of the head when viewed from above. https://wdfw.wa.gov/species-habitats/species/pseudacris-regilla
Western toad tadpoles are black dorsally and, ventrally, have minimal if any metallic flecking, have flattened bodies, have a tail fin that does not extend onto the back, and have narrowly placed dorsal eyes on top of the head.
Large American bullfrog and American green frog tadpoles have distinct black spots on a khaki-colored body and the abdomen is an opaque yellow (intestines not visible) with no metallic pigment (bullfrog) or with a coppery sheen (green frog).
Eggs
Egg masses are globular with jelly that is soft and pliable to the touch. Roughly the size of a grapefruit, they are attached to vegetation 6 inches or more below the water surface. Newly laid eggs appear black on top and white on the bottom. As the embryos develop, the jelly becomes looser and the egg mass tends to break free of its attachment, often flattening out and floating to the surface. Newly hatched tadpoles disperse from the egg mass soon after hatching.
The Cascades frog, Oregon spotted frog and Columbia spotted frog typically lay their eggs in communal clusters that consist of many (up to 60 or more) egg masses laid next to or on top of each other in shallow (less than 6 inches) water and the eggs are not attached to sticks or vegetation.
The northwestern salamander has a fist-sized globular egg mass that is solid to the touch, always attached to vegetation and the animal pole of the egg and the embryos are brown not black or dark brown.
Voice
The advertisement call is a weak, stuttering set of guttural notes (4 to 7) given on one pitch “uh-uh-uh-uh.” This call, produced primarily underwater, requires one to be close to the calling male to hear it. A chorus sounds like soft “clucking.” Individual males also produce infrequent low volume calls, “chuckles,” from terrestrial sites during the active season. The release call is “chuckling” accompanied by pulsing of the body. When grabbed by certain predators, such as common garter snakes, northern red-legged frogs release a loud and startling “scream.” Listen to the calls of northern red-legged frog in this short audio clip.
For more details about red-legged frog, see the Washington Herp Atlas.
Ecology and life history
Northern red-legged frogs are found in lowland (mostly below 3000 feet in Washington) moist forested habitats with access to suitable breeding sites. This species can persist in areas of low-density development and landscapes managed for timber. Transformed northern red-legged frogs are the most terrestrial of our native True Frogs. It is not unusual to find them in moist forested habitats far from water bodies. However, most individuals are found in the vicinity of standing or flowing water, even during the non-breeding terrestrial phase of the seasonal life cycle. Juveniles have been found in road puddles in disturbed open habitats that would not typically be considered suitable habitat for the species. Puddles and other temporary sources of standing water may be important features for dispersing individuals.
The few data obtained on overwintering for northern red-legged frogs in the Puget Lowlands of Washington have revealed that the species may overwinter in terrestrial habitat at least for part of the season. Overwintering data from the lower Columbia in Oregon indicate that frogs will shuttle between aquatic and terrestrial habitat depending on wintertime temperatures, moving into water when conditions are colder. Regardless of precise overwintering location, this species can remain active throughout the winter at low-elevation sites except when temperatures are near or below freezing.
During periods of inactivity, northern red-legged frogs have been found sheltering under or within sword fern fronds, the duff that accumulates below sword ferns, under woody debris and within stream banks.
Northern red-legged frogs can be active both day and night depending on temperature; during wet intervals, most activity takes place at night. They blend well into their surroundings and are difficult to detect unless they move. They are alert, fast frogs that will remain motionless when approached and then suddenly flee by leaping away with relatively long but evasive jumps.
Breeding habitats include a variety of still-water bodies that generally persist until at least July at low elevations, later at high elevations. Vegetation suitable for egg mass attachment must typically also be present. However, northern red-legged frogs can sometimes lay eggs in mud puddles with no attachment brace, but this pattern is infrequent. Larvae are grazers and can strongly influence the distribution of algae (periphyton) in some still-water habitats. In water bodies with introduced warm-water fish, egg masses are uncommon or absent suggesting that northern red-legged frogs avoid these water bodies for egg laying.
Breeding in Thurston County, at 50 to 100 feet elevation, starts in late January or early February. Most eggs are laid within 2 to 3 weeks at each site, but a small percentage of populations, especially large ones, will continue to lay over a longer period of time. In southwestern British Columbia, eggs take approximately 3 to 5 weeks to hatch depending on when they are laid, water depth and water temperature. Oviposition appears to occur when surface water temperatures have reached 43° Fahrenheit. Most egg masses have hatched by late March in lowland areas. Tadpoles at low elevations start to transform in late June of their first year.
Experimental studies have revealed that exotic warm-water fishes can interact with bullfrogs and other aquatic fauna in a manner that produces negative effects on northern red-legged frogs. Overall, however, habitat structure and the presence of exotic fishes appear to be more important in determining the overall distribution and abundance of northern red-legged frogs than simply the presence of American bullfrogs.
Geographic range
In Washington, northern red-legged frogs occur in the Pacific Coast, Puget Trough, North Cascades, West Cascades and East Cascades ecoregions. East of the Cascade crest, the only records from Kittitas and Yakima Counties are old museum specimen records.
This map from the Washington Herp Atlas illustrates the distribution of northern red-legged frog in Washington based on records in the WDFW database as of 2016. If you see this species in areas that are not indicated on the map or have more recent observations (less than 10 years), please share your observation using the WDFW wildlife reporting form.
For a map of range-wide distribution and conservation status of this species, check out NatureServe Explorer and the International Union for Conservation of Nature Redlist.
Regulations
Licenses and permits
Be advised that collection of this species is only permitted under a WDFW Scientific Collection Permit for research and educational activities.
Conservation
The state conservation status of the northern red-legged frog is “apparently secure” based on the assumption that it is common according to the most current records.
Substantial recent declines have been documented for this species in other states. Reasons for the declines, other than habitat loss and alteration, have not been confirmed but have been attributed to impacts of introduced fishes, introduced American bullfrogs, hydrology, endocrine disruptors, nitrogen compounds, and toxicants. In some cases, as for UV radiation, experimental work found no mortality but negative sub-lethal effects may exist. Among the least studied threats, that is coupled with increased urbanization, is road mortality.
Monitoring of populations is recommended, particularly in landscapes that are rapidly being urbanized as this species may be able to survive only in situations with intermediate levels of urbanization at best. Breeding sites should be monitored regularly to make sure that populations are persisting even with substantial habitat loss across the Puget Trough; an area that covers roughly one-third of northern red-legged frog range in Washington. Annual egg mass surveys to determine number of breeding females (one egg mass per adult female) is the most efficient method for monitoring populations of this species for long-term trend analyses. Early March is the best time to survey for egg masses of lowland populations.
Despite advances in research, fully understanding the spatial scale at which this species operates both seasonal and inter-seasonally under different habitat conditions remains a significant knowledge gap in this species’ biology. More research in this area, and addressing overwintering patterns, is especially needed.
Research using genetic data has resulted in a systematic revision of red-legged frogs (Shaffer et al. 2004) revealing that not only are northern and California red-legged frogs valid species, but they are not closest relatives as previously thought. Apparently, northern red-legged frogs are more closely related to Cascades frogs than they are to California red-legged frogs. This has important implication to understanding the biology of northern red-legged frogs and defining the status of the species within different states and provinces.
Living with wildlife
Frogs, along with salamanders and newts, are members of the animal group called amphibians. Frogs start their lives as totally aquatic larvae with gills and a pronounced tail fin; this is familiar to many people as the tadpole stage. Over time, legs develop, the tail and gills are absorbed, and the frog transforms into a terrestrial, air-breathing animal.
Learn more about living with frogs, including how to attract them or prevent conflicts.
Resources
References
Adams, M. J. 1999. Correlational factors in amphibian declines: Exotic species and habitat change in western Washington. Journal of Wildlife Management 63(4):1162-1171.
Adams, M. J., C. A. Pearl, and R. B. Bury. 2003. Indirect facilitation of an anuran invasion by non-native fishes. Ecology Letters 6(4): 343-351.
Beasley, B.A. 2002. The SPLAT Project: Monitoring amphibian movements and mortality on a highway crossing the coastal flats of Clayoquot, British Columbia. Northwestern Naturalist 83:64. [abstract]
Belden, L.K., and A. R. Blaustein. 2002. Exposure of red-legged frog embryos to ambient UV-B in the field negatively affects larval growth and development. Oecologia 130:551–554.
Bettaso, J. B., H. H. Welsh Jr., and B. D. Palmer. 2002. Northern red-legged frogs and endocrine disrupting compounds (EDCs). Froglog 52:1.
Brown, H. A. 1975. Reproduction and development of the red-legged frog, Rana aurora, in northwestern Washington. Northwest Science. 49:241-252.
Calef, G. W. 1973a. Spatial distribution and effective breeding population of red-legged frogs (Rana aurora) in Marion Lake, British Columbia. Canadian Field-Naturalist 87:279-284.
Calef, G. W. 1973b. Natural mortality of tadpoles in a population of Rana aurora. Ecology 54:741-758.
Callison, C. M. 2001. Factors influencing oviposition among pond-breeding amphibians: Exotic vegetation, oviposition braces, and cover. Unpubl. master’s thesis. Portland State University, Portland, OR.
Chan-McLeod, A. A. 2003. Factors affecting the permeability of clearcuts to red-legged frogs. Journal of Wildlife Management 67:663-671.
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Haggard, J. A. 2000. A radio telemetric study of the movement patterns of adult northern red-legged frogs (Rana aurora aurora) at Freshwater Lagoon, Humboldt County, California. Unpubl. master’s thesis. Humboldt State University, Arcata, CA.
Hayes, M. P., and C. B. Hayes. 2003. Rana aurora aurora: Juvenile growth; Male size at maturity. Herpetological Review 34:233-234.
Hayes, M. P. and M.R. Jennings. 1986. Decline of ranid frogs species in Western North America: Are Bullfrogs (Rana catesbeiana) responsible? Journal of Herpetology 20 (4): 490-509.
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Kiesecker, J. M., and A. R. Blaustein. 1998. Effects of introduced bullfrogs and smallmouth bass on microhabitat use, growth, and survival of native red-legged frogs (Rana aurora). Conservation Biology 12:776-787.
Leonard, W.P., K.R. McAllister, L.A. Hallock. 1997. Autumn vocalizations by the red-legged frog (Rana aurora) and the Oregon spotted frog (Rana pretiosa). Northwestern Naturalist 78:73-74.
Licht, L. E. 1969. Comparative breeding behavior of the red-legged frog (Rana aurora aurora) and the western spotted frog (Rana pretiosa pretiosa) in southwestern British Columbia. Canadian Journal of Zoology 47:1287-1299.
Licht, L. E. 1969. Palatability of Rana and Hyla eggs. American Midland Naturalist 82:296-298.
Licht, L. E. 1971. Breeding habits and embryonic thermal requirements of the frogs Rana aurora aurora and Rana pretiosa pretiosa in the Pacific Northwest. Ecology 52:116-124.
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Licht, L. E. 1986. Comparative escape behavior of sympatric Rana aurora and Rana pretiosa. American Midland Naturalist 115:239-247.
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Pearl, C. A., M. J. Adams, R. B. Bury, and B. McCreary. 2004. Asymmetrical effects of introduced bullfrogs (Rana catesbeiana) on native ranid frogs in Oregon. Copeia 2004:11-20.
Pearl, C. A., M. P. Hayes, R. Haycock, J. D. Engler, and J. Bowerman. 2005. Observations of interspecific amplexus between western North American ranid frogs and the introduced American bullfrog (Rana catesbeiana) and an hypothesis concerning breeding interference. American Midland Naturalist 154:126-134.
Pearl, C. A., M. J. Adams, N. Leuthold, and R. B. Bury. 2005b. Amphibians occurrence and aquatic invaders in a changing landscape: Implications for wetland mitigation in the Willamette Valley, Oregon, USA. Wetlands 25:76-88.
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Richter, K. O., and A. L. Azous. 2001. Amphibian distribution, abundance, and habitat use. p.143-165. In A. L. Azous and R. R. Horner (eds.) Wetlands and Urbanization: Implications for the Future. Lewis Publishers, Boca Raton, FL.
Ritson, P. E., and M. P. Hayes. 2000. Late season activity and overwintering in the northern red-legged frog (Rana aurora aurora). Final report to the U.S. Fish and Wildlife Service. Portland, OR.
Shaffer, H. B., G. M. Fellers, S. R. Voss, J. C. Oliver, and G. B. Pauly. 2004. Species boundaries, phylogeography and conservation genetics of the red-legged frog (Rana aurora/draytonii) complex. Molecular Ecology 13:2667-2677.
Schuett-Hames, J. P. 2004. Northern red-legged frog (Rana aurora aurora) terrestrial habitat use in the Puget Lowlands of Washington. Unpubl. master’s thesis. The Evergreen State College, Olympia, WA.
Schuytema, G. S., and A. V. Nebeker. 1996. Amphibian Toxicity Data for Water Quality Criteria Chemicals. U.S. Environmental Protection Agency, National Health Environmental Research Laboratory, Western Ecology Division, Corvallis, OR.
Schuytema, G. S., and A. V. Nebeker. 1998. Comparative toxicity of diuron on survival and growth of Pacific treefrog, bullfrog, red-legged frog, and African clawed frog embryos and tadpoles. Archives of Environmental Contamination and Toxicology 34:370-376.
Schuytema, G. S., and A. V. Nebeker. 1999. Effects of ammonium nitrate, sodium nitrate and urea red-legged frogs, Pacific treefrogs and African clawed frogs. Bulletin of Environmental Contamination and Toxicology 63:357-364.
Serra Shean, J. T. 2002. Post-breeding movements and habitat use by the northern red-legged frog, Rana aurora aurora, at Dempsey Creek, Thurston County, Washington. Unpubl. master’s thesis, The Evergreen State College, Olympia, WA.
Storm, R.M. 1960. Notes on the breeding biology of the red-legged frog (Rana aurora aurora). Herpetologica 16:251-259.
Twedt, B. K. 1993. A comparative ecology of Rana aurora Baird and Girard and Rana catesbeiana Shaw at Freshwater Lagoon, Humboldt County, California. Unpubl. master’s thesis, Humboldt State University, Arcata, California.
Personal communications
Marc Hayes, Washington Department of Fish and Wildlife, Olympia, Washington.
Tuesday Serra Shean, The Evergreen State University (2002 Master’s Thesis), Olympia, Washington.
Joanne Schuett-Hames, Washington Department of Fish and Wildlife, Olympia, Washington
WDFW publications
WDFW educational resources
- Wild Washington Lesson Plan – Herps in Washington - Elementary school students are introduced to the cold-blooded world of reptiles and amphibians, also known as herps.
- Family Education – Amphibians and Reptiles - Slither, hop, or crawl on over to learn about herpetofauna!